ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS
K-Number: K903292 · 1990-10-19
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Device Summary
Frequently Asked Questions
What is the ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS?
ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Coe Laboratories, Inc.. The 510(k) number is K903292.
When did ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS receive FDA 510(k) clearance?
ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS received FDA 510(k) clearance on 1990-10-19, under 510(k) number K903292.
Who is the listed applicant for ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS?
The FDA 510(k) record lists Coe Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS?
The FDA product code for ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS is ELW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Coe Laboratories, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ELW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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